Variant #0000849846 (NC_000002.11:g.27601437G>A, NM_144631.5:c.696C>T (ZNF513))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27601437G>A
DNA change (hg38) -
Published as ZNF513(NM_144631.6):c.696C>T (p.P232=)
ISCN -
DB-ID PPM1G_000018
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00019 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNX17 NM_014748.3 -?/. - c.*1851G>A r.(=) p.(=)
ZNF513 NM_144631.5 -?/. - c.696C>T r.(?) p.(Pro232=)
PPM1G NM_177983.2 -?/. - c.*3029C>T r.(=) p.(=)


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